IL217285A - (s)-enantiomer of a spiro-oxindole compound and its uses in the manufacture of a medicament for decreasing ion flux through voltage-gated sodium channel - Google Patents
(s)-enantiomer of a spiro-oxindole compound and its uses in the manufacture of a medicament for decreasing ion flux through voltage-gated sodium channelInfo
- Publication number
- IL217285A IL217285A IL217285A IL21728511A IL217285A IL 217285 A IL217285 A IL 217285A IL 217285 A IL217285 A IL 217285A IL 21728511 A IL21728511 A IL 21728511A IL 217285 A IL217285 A IL 217285A
- Authority
- IL
- Israel
- Prior art keywords
- enantiomer
- spiro
- medicament
- manufacture
- voltage
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/20—Spiro-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
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- A61P13/10—Drugs for disorders of the urinary system of the bladder
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P3/06—Antihyperlipidemics
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- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B57/00—Separation of optically-active compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/22—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US22142409P | 2009-06-29 | 2009-06-29 | |
PCT/US2010/040187 WO2011002708A1 (en) | 2009-06-29 | 2010-06-28 | Enantiomers of spiro-oxindole compounds and their uses as therapeutic agents |
Publications (2)
Publication Number | Publication Date |
---|---|
IL217285A0 IL217285A0 (en) | 2012-02-29 |
IL217285A true IL217285A (en) | 2016-09-29 |
Family
ID=42416878
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IL217285A IL217285A (en) | 2009-06-29 | 2011-12-29 | (s)-enantiomer of a spiro-oxindole compound and its uses in the manufacture of a medicament for decreasing ion flux through voltage-gated sodium channel |
IL241985A IL241985A (en) | 2009-06-29 | 2015-10-08 | Process of preparing (s)- enantiomer of a spiro-oxindole compound |
IL250314A IL250314A0 (en) | 2009-06-29 | 2017-01-26 | Enantiomers of spiro-oxindole compounds and their uses as therapeutic agents |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IL241985A IL241985A (en) | 2009-06-29 | 2015-10-08 | Process of preparing (s)- enantiomer of a spiro-oxindole compound |
IL250314A IL250314A0 (en) | 2009-06-29 | 2017-01-26 | Enantiomers of spiro-oxindole compounds and their uses as therapeutic agents |
Country Status (35)
Country | Link |
---|---|
US (4) | US8450358B2 (en) |
EP (3) | EP2448943B1 (en) |
JP (3) | JP2012532107A (en) |
KR (1) | KR101751378B1 (en) |
CN (2) | CN104650106A (en) |
AR (1) | AR077252A1 (en) |
AU (1) | AU2010266549B2 (en) |
BR (1) | BRPI1012129A2 (en) |
CA (1) | CA2764878C (en) |
CL (1) | CL2011003335A1 (en) |
CO (1) | CO6470866A2 (en) |
CY (1) | CY1117776T1 (en) |
DK (1) | DK2448943T3 (en) |
EC (1) | ECSP11011512A (en) |
ES (2) | ES2578779T3 (en) |
HK (2) | HK1168854A1 (en) |
HR (2) | HRP20110946A2 (en) |
HU (1) | HUE029658T2 (en) |
IL (3) | IL217285A (en) |
MA (1) | MA33552B1 (en) |
MX (2) | MX2012000028A (en) |
MY (1) | MY159099A (en) |
NZ (1) | NZ596903A (en) |
PE (2) | PE20120413A1 (en) |
PH (1) | PH12015502323A1 (en) |
PL (2) | PL2448943T3 (en) |
PT (1) | PT2448943T (en) |
RU (1) | RU2535667C2 (en) |
SG (1) | SG176307A1 (en) |
SI (1) | SI2448943T1 (en) |
SM (1) | SMT201600203B (en) |
TN (1) | TN2011000664A1 (en) |
TW (1) | TWI465452B (en) |
WO (1) | WO2011002708A1 (en) |
ZA (1) | ZA201108960B (en) |
Families Citing this family (64)
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US9278088B2 (en) | 2002-02-19 | 2016-03-08 | Xenon Pharmaceuticals Inc. | Methods for identifying analgesic agents |
AR053710A1 (en) * | 2005-04-11 | 2007-05-16 | Xenon Pharmaceuticals Inc | SPIROHETEROCICLIC COMPOUNDS AND THEIR USES AS THERAPEUTIC AGENTS |
MY158766A (en) * | 2005-04-11 | 2016-11-15 | Xenon Pharmaceuticals Inc | Spiro-oxindole compounds and their uses as therapeutic agents |
BRPI0719210A2 (en) | 2006-10-12 | 2015-05-05 | Xenon Pharmaceuticals Inc | Use of spiro-oxindole compounds as therapeutic agents |
EP2076514A1 (en) * | 2006-10-12 | 2009-07-08 | Xenon Pharmaceuticals Inc. | Spiro (furo ý3, 2-c¨pyridine-3-3 ' -indol) -2' (1'h)-one derivatives and related compounds for the treatment of sodium-channel mediated diseases, such as pain |
US8101647B2 (en) * | 2008-10-17 | 2012-01-24 | Xenon Pharmaceuticals Inc. | Spiro-oxindole compounds and their use as therapeutic agents |
SG10201703082XA (en) | 2008-10-17 | 2017-06-29 | Xenon Pharmaceuticals Inc | Spiro-oxindole compounds and their use as therapeutic agents |
AR077252A1 (en) | 2009-06-29 | 2011-08-10 | Xenon Pharmaceuticals Inc | ESPIROOXINDOL COMPOUND ENANTIOMERS AND THEIR USES AS THERAPEUTIC AGENTS |
MX2011013816A (en) | 2009-06-29 | 2012-04-11 | Incyte Corp | Pyrimidinones as pi3k inhibitors. |
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WO2011075643A1 (en) | 2009-12-18 | 2011-06-23 | Incyte Corporation | Substituted heteroaryl fused derivatives as pi3k inhibitors |
WO2011106729A2 (en) * | 2010-02-26 | 2011-09-01 | Xenon Pharmaceuticals Inc. | Pharmaceutical compositions of spiro-oxindole compound for topical administration and their use as therapeutic agents |
WO2011130342A1 (en) | 2010-04-14 | 2011-10-20 | Incyte Corporation | FUSED DERIVATIVES AS ΡI3Κδ INHIBITORS |
US9062055B2 (en) | 2010-06-21 | 2015-06-23 | Incyte Corporation | Fused pyrrole derivatives as PI3K inhibitors |
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US9108984B2 (en) | 2011-03-14 | 2015-08-18 | Incyte Corporation | Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors |
US9126948B2 (en) | 2011-03-25 | 2015-09-08 | Incyte Holdings Corporation | Pyrimidine-4,6-diamine derivatives as PI3K inhibitors |
MY179332A (en) | 2011-09-02 | 2020-11-04 | Incyte Holdings Corp | Heterocyclylamines as pl3k inhibitors |
EP2638908A1 (en) * | 2012-03-16 | 2013-09-18 | Phytotox SpA | Paralytic Shellfish Poison |
AR090548A1 (en) | 2012-04-02 | 2014-11-19 | Incyte Corp | BICYCLIC AZAHETEROCICLOBENCILAMINS AS PI3K INHIBITORS |
US9487535B2 (en) | 2012-04-12 | 2016-11-08 | Xenon Pharmaceuticals Inc. | Asymmetric syntheses for spiro-oxindole compounds useful as therapeutic agents |
GB201209015D0 (en) * | 2012-05-22 | 2012-07-04 | Convergence Pharmaceuticals | Novel compounds |
CA2901208A1 (en) * | 2013-02-13 | 2014-08-21 | Novartis Ag | Topical ocular analgesic agents |
RU2692766C1 (en) | 2013-12-13 | 2019-06-27 | Вертекс Фармасьютикалз Инкорпорейтед | Prodrugs of pyridonamides used as modulators of sodium channels |
US20150216794A1 (en) * | 2014-02-05 | 2015-08-06 | IVAX International GmbH | Methods of treating pain associated with osteoarthritis of a joint with a topical formulation of a spiro-oxindole compound |
WO2015151001A1 (en) | 2014-03-29 | 2015-10-08 | Lupin Limited | Sulfonamide compounds as voltage gated sodium channel modulators |
US10077277B2 (en) | 2014-06-11 | 2018-09-18 | Incyte Corporation | Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors |
WO2016109795A1 (en) | 2014-12-31 | 2016-07-07 | Concert Pharmaceuticals, Inc. | Deuterated funapide and difluorofunapide |
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